MLI SOFT TISSUE SCREW & WASHER SYSTEM

MLI SOFT TISSUE SCREW & WASHER SYSTEM is an FDA 510(k)-cleared medical device (K962194) manufactured by Medicinelodge, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 29, 1996. Regulation: 8.